Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61725028-61725278 | Common:1; Rare:118 | ||||
chr1:62688271-62688504 | Common:1; Rare:96 | ||||
chr1:63523192-63523563 | Common:3; Rare:93 | ||||
chr1:63593163-63593456 | Rare:102; Clinvar (benign):1 | ||||
chr1:66332236-66332459 | Rare:61 | ||||
chr1:66924851-66925024 | Rare:75 | ||||
chr1:67053934-67054026 | Rare:41 | ||||
chr1:67430131-67430582 | Rare:165 | ||||
chr1:70205487-70205759 | Rare:101 | ||||
chr1:70221303-70221506 | Rare:86 | ||||
chr1:70354674-70354838 | Rare:58 | ||||
chr1:70411100-70411271 | Rare:40; Clinvar:1 | ||||
chr1:71080956-71081364 | Rare:110 | ||||
chr1:72282669-72282973 | Common:4; Rare:88 | ||||
chr1:74198174-74198270 | Rare:56 |